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Results 31 - 40 of 103 for Abnormal embryonic development
  1. Recurrent hydatidiform mole 
    ... for normal egg cell (oocyte) development, which impacts embryonic development. Within oocytes, the exact role of NLRP7 and ... that contribute to a developing embryo, leading to abnormal gene activity ... contribute to the development of a hydatidiform mole. In women with NLRP7 ...
    https://medlineplus.gov/.../condition/recurrent-hydatidiform-mole - Genetics
  2. Terminal osseous dysplasia 
    ... be lethal very early in development. Early in embryonic development in females, one of the two X chromosomes ...
    https://medlineplus.gov/.../condition/terminal-osseous-dysplasia - Genetics
  3. White-Sutton syndrome 
    ... reproductive cells (eggs or sperm) or in early embryonic development. Mental retardation, autosomal dominant 37 MRD37 WHSUS Genetic ...
    https://medlineplus.gov/genetics/condition/white-sutton-syndrome - Genetics
  4. Congenital hypothyroidism 
    ... reproductive cells (eggs or sperm) or in early embryonic development. These cases occur in people with no history ...
    https://medlineplus.gov/genetics/condition/congenital-hypothyroidism - Genetics
  5. 46,XX testicular difference of sex development 
    ... reproductive cells (eggs or sperm) or in early embryonic development. These cases occur in people with no history ...
    https://medlineplus.gov/...-testicular-difference-of-sex-development - Genetics
  6. Poland syndrome 
    ... to occur at about the sixth week of embryonic development and affect blood vessels that will become the ... that occur in Poland syndrome. Abnormality of an embryonic structure called the apical ectodermal ridge, which helps direct early limb development, may also be involved in this disorder.Rare ...
    https://medlineplus.gov/genetics/condition/poland-syndrome - Genetics
  7. GRIN2B-related neurodevelopmental disorder 
    ... an affected individual's parent or in early embryonic development. These cases occur in people with no history ...
    https://medlineplus.gov/...rin2b-related-neurodevelopmental-disorder - Genetics
  8. Paroxysmal nocturnal hemoglobinuria 
    ... Females have two X chromosomes. However, early in embryonic development in females, one of the two X chromosomes ...
    https://medlineplus.gov/.../paroxysmal-nocturnal-hemoglobinuria - Genetics
  9. X-linked myotubular myopathy 
    ... reproductive cells (eggs or sperm) or in early embryonic development. Females with one altered copy of the MTM1 ...
    https://medlineplus.gov/.../condition/x-linked-myotubular-myopathy - Genetics
  10. Kniest dysplasia 
    ... an affected individual's parent or during early embryonic development. These affected individuals often have no history of ...
    https://medlineplus.gov/genetics/condition/kniest-dysplasia - Genetics
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